Canonical Allele Identifier: PA2825160897
Gene: WT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 579939

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000369.4:p.Gln160His
CA379964936
NM_000378.6:c.480G>T
CA379964937
NM_000378.6:c.480G>C